نتایج جستجو برای: ژن nd1

تعداد نتایج: 16327  

Journal: :Molecular phylogenetics and evolution 2006
Miquel A Arnedo Rosemary G Gillespie

Hotspot archipelagoes provide exceptional models for the study of the evolutionary process, due to the effects of isolation and topographical diversity in inducing the formation of unique biotic assemblages. In this paper, we examine the evolutionary patterns exhibited by the jumping spider genus Havaika Prószyński, 2001 in the Polynesian islands of the Hawaiian and Marquesas chains. To date, s...

2017
Jessica Rach Tjard Bergmann Omid Paknia Rob DeSalle Bernd Schierwater Heike Hadrys

The potential of DNA barcoding approaches to identify single species and characterize species compositions strongly depends on the marker choice. The prominent "Folmer region", a 648 basepair fragment at the 5' end of the mitochondrial CO1 gene, has been traditionally applied as a universal DNA barcoding region for metazoans. In order to find a suitable marker for biomonitoring odonates (dragon...

Journal: :Molecular phylogenetics and evolution 2001
M C Hedin W P Maddison

Four gene regions were sequenced for 30 species of jumping spiders, most from the subfamily Dendryphantinae, to investigate their molecular phylogeny and evolution. These are three regions from the mitochondria (ca. 560 bp of 16S plus adjacent tRNA, 1047 bp of cytochrome oxidase 1 (CO1), and 414 bp of NADH1 (ND1) and one region from the nuclear genome (ca. 750 bp of 28S). Parsimony and likeliho...

Journal: :Therapeutics and clinical risk management 2016
Maryam Balali Behnam Kamalidehghan Mohammad Farhadi Fatemeh Ahmadipour Mahmoud Dehghani Ashkezari Mohsen Rezaei Hemami Hossein Arabzadeh Masoumeh Falah Goh Yong Meng Massoud Houshmand

Mitochondrial DNA mutations play an important role in causing sensorineural hearing loss. The purpose of this study was to determine the association of the mitochondrial genes RNR1, MT-TL1, and ND1 as well as the nuclear genes GJB2 and GJB6 with audiological examinations in nonfamilial Iranians with cochlear implants, using polymerase chain reaction, DNA sequencing, and RNA secondary structure ...

Journal: :The Malaysian journal of pathology 2010
Yakob Yusnita Md Desa Norsiah A Jamal Rahman

Mitochondrial Subunit ND1 (mtND1) gene is involved in the first step of the electron transport chain of oxidative phosphorylation (OXPHOS). Alteration of the electron transport components by mutations in mtDNA may compromise the normal electron flow. This could lead to an increase of bifurcation and generation of superoxidase radicals and increase oxidative stress in various types of cancer cel...

Journal: :Gene 2008
Lalani Yatawara Thanh Hoa Le Susiji Wickramasinghe Takeshi Agatsuma

We report 8420 bp of DNA sequence data from the maxicircle (mitochondrial) genome of Leishmania major (MHOM/SU/73/5ASKH), a much larger portion of this genome than has been reported previously from any Leishmania species infecting humans. This region contains 10 partial and complete genes: 5 protein-encoding genes (COII, COIII, ND1, ND7 and Cyt b); two ribosomal RNA subunits (12S and 9S) and th...

Journal: :Acta Crystallographica Section A Foundations of Crystallography 2008

2017
Weiyang Li Yanwei Qi Xiaofang Cui Yuhui Sun Qing Huo Yan Yang Xinyuan Wen Meihua Tan Shiyi Du Huali Zhang Meng Zhang Chuanxin Liu Qingsheng Kong

Hepatocellular carcinoma (HCC) is the third leading cause of cancer mortality worldwide. In this study, we had analysed the copy number variations and heteroplasmic mutations of mitochondria (MT) in 88 HCC individuals. The average copy number of MT genome in normal samples was significantly greater than that in tumor samples. Overall, the number of heteroplasmic mutations in 88 tumor and their ...

Journal: :Nucleic acids research 2004
Xiaoming Li Nathan Fischel-Ghodsian Faina Schwartz Qingfeng Yan Rick A Friedman Min-Xin Guan

We report here the biochemical characterization of the deafness-associated mitochondrial tRNA(Ser(UCN)) T7511C mutation, in conjunction with homoplasmic ND1 T3308C and tRNA(Ala) T5655C mutations using cybrids constructed by transferring mitochondria from lymphoblastoid cell lines derived from an African family into human mtDNA-less (rho degrees ) cells. Three cybrids derived from an affected ma...

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